| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217133 | Tetrahedron | 2014 | 5 Pages |
Abstract
A simple, practical, and regioselective synthetic protocol for the formation of pyrazoles was developed. Unlike all other previously reported reactions of nitroallylic acetates, this process was initiated by a SN2 reaction at the electrophilic γ site. A plausible mechanism for the cascade SN2-Michael synthesis is proposed.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
